分子标记在食用菌鉴定中的应用——以银耳为例

Jing-Gung Chung, J. Tsai, Chien-Yih Lin, Yang-Chia Shih, Jin-Shih Chen, M. Fan
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引用次数: 1

摘要

不同银耳(Tremella fuciformis Berk)品种具有不同的形态和产量潜力。为了进行种间鉴定,利用BM36和BM37引物生成内部转录间隔序列(internal transcript spacer, ITS)进行测序。结果表明,黑木耳、银耳和弓形木耳分别在570 bp、470 bp和860 bp处存在不同的条带。在不同地区采集的7个品种中,姬松茸和灰树花的分子带均为710 bp,灰树花的分子带均为630 bp。结果表明,ITS可作为种间分子标记,但不能作为种内分子标记。对银耳品种产生的条带进行测序,发现相似性达99%,差异多为单核苷酸多态性(SNP),通过ITS方法能找到的分子标记很少。本研究建立了一种结合自适应连接PCR和抑制PCR的双抑制PCR方法,生成SSR (simple sequence repeat)引物集。利用该方法设计的特殊引物组,可以通过对PCR产物进行测序来检测SSR。目前,我们有3套引物可作为银耳品种鉴定的分子标记,并通过测序结果进行了验证。结果表明,BM66和BM93引物对LT1、LT2、LT4、LT6的SSR序列为(AG) 14,对LT7、LT12的SSR序列为(AG) 13。引物设置BM67和BM92产生的SSR序列:lt1和LT4为(C)14(T)18, LT2为(C)15(T)16, LT6为(C)13(T)19, LT7为(C)14(T)16, LT12为(C)12(T)19。引物组BM99和BM102的结果表明,本研究中使用的银耳品种可以区分为两组。LT1、LT2和LT7的DNA序列为tgt,而不是在LT4、LT6和LT12组中替换的gtctccatttgt。结果表明,银耳种在种内的差异很小,但本研究采用的方法可以区分银耳品种。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Application of Molecular Markers to Identify Edible Fungi: A Case Study of Tremella Fuciformis
Different Tremella fuciformis Berk (TFB) cultivars have different morphology and yield potential. For the identification of interspecies, the internal transcript spacer (ITS) sequences were generated by primers set BM36 and BM37 then sequenced. The results showed different bands at 570 bp for Auricularia auricula, 470 bp for Tremella fuciformis and 860 bp for Hypoxylon archeri. Among seven cultivars of Agaricus Blazei or Grifola frondosa which we collected from different area, they show same molecular bands by ITS method, 710 bp for all seven varieties Agaricus Blazei and 630 bp for all seven varieties of Grifola frondosa. The results showed that ITS can be used as an interspecies molecular marker while not for intraspecies. After sequence those bands generated by Tremella fuciformis cultivars, 99% similarity were found, and most of the different are single nucleotide polymorphism (SNP), very few molecular marker can be found by ITS method. A dual-suppression PCR method combine with adaptorligation PCR and suppression PCR were developed by this research to generate the primers set for SSR (simple sequence repeat). By using this method, the SSR can be detected by sequence the PCR products when using the special primers set design by this method. Currently, we have three primers sets can be used as molecular marker for Tremella fuciformis cultivars identification and the results had been confirmed by sequencing. The result shows that BM66 and BM93 primers set can generate SSR sequence: (AG) 14 for LT1, LT2, LT4, LT6 and SSR sequence: (AG) 13 for LT7, LT12. The primers set BM67 and BM92 generated SSR sequence: (C)14(T)18 forLT1 and LT4, (C)15(T)16 for LT2, (C)13(T)19 for LT6, (C)14(T)16 for LT7 and (C)12(T)19 for LT12. The result of primers set BM99 and BM102 showed two groups of the cultivar of Tremella fuciformis used in this research can be distinguished. The LT1, LT2 and LT7 belong to one group by DNA sequence tgt instead of gtctccatttgt which is replace in group LT4, LT6 and LT12. The result shows even it is very tiny different in intraspecies of Tremella fuciformis, but the methods which we used in this research can distinguish those cultivars.
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